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A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
- Correspondence to Dr Alison M Elliott, Departments of Pediatrics and Child Health; Biochemistry and Medical Genetics, University of Manitoba, Faculty of Medicine, FE229 CSB, 820 Sherbrook Street, Winnipeg, MB, Canada R3A 1R9; aelliott{at}hsc.mb.ca; and Dr Louise R Simard, Departments of Pediatrics and Child Health; Biochemistry and Medical Genetics, University of Manitoba, Faculty of Medicine, 312 Basic Medical Sciences Building, 745 Bannatyne Avenue, Winnipeg, MB, Canada R3E 0J9; Louise.Simard{at}med.umanitoba.ca
Citation
A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
Publication history
- Received April 4, 2013
- Revised August 3, 2013
- Accepted August 28, 2013
- First published September 24, 2013.
Online issue publication
November 05, 2013
Article Versions
- Previous version (24 September 2013).
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